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rs3098019

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs3098019(G;T)
Make rs3098019(T;T)
ReferenceGRCh38 38.1/142
Chromosome6
Position29943494
GeneHLA-A
is asnp
is mentioned by
dbSNPrs3098019
ebirs3098019
HLIrs3098019
Exacrs3098019
Varsomers3098019
Maprs3098019
PheGenIrs3098019
hapmaprs3098019
1000 genomesrs3098019
hgdprs3098019
ensemblrs3098019
gopubmedrs3098019
geneviewrs3098019
scholarrs3098019
googlers3098019
pharmgkbrs3098019
gwascentralrs3098019
openSNPrs3098019
23andMers3098019
23andMe allrs3098019
SNP Nexus

SNPshotrs3098019
SNPdbers3098019
MSV3drs3098019
GWAS Ctlgrs3098019
GMAF0.1919
Max Magnitude0
ClinVar
Risk rs3098019(A,C,T;A,C,T)
Alt rs3098019(A,C,T;A,C,T)
Reference rs3098019(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29911271G>A; NC_000006.11:g.29911271G>C; NC_000006.11:g.29911271G>T
CLNSRC
CLNACC